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    Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

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    Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.

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    Micafungin Sodium

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    01 2APOTEX

    02 2ASTELLAS

    03 3BAXTER HLTHCARE CORP

    04 2BIOCON PHARMA

    05 2ENDO OPERATIONS

    06 2FRESENIUS KABI USA

    07 1FUJISAWA HLTHCARE

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    01

    APOTEX

    Canada
    Pharma, Lab & Chemical Expo
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    APOTEX

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    RLD : No

    TE Code :

    MICAFUNGIN SODIUM

    Brand Name : MICAFUNGIN SODIUM

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : EQ 50MG BASE/VIAL

    Approval Date : 2020-11-05

    Application Number : 208366

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    APOTEX

    Canada
    Pharma, Lab & Chemical Expo
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    APOTEX

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    RLD : No

    TE Code :

    MICAFUNGIN SODIUM

    Brand Name : MICAFUNGIN SODIUM

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

    Approval Date : 2020-11-05

    Application Number : 208366

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    ASTELLAS

    Japan
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    ASTELLAS

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    RLD : Yes

    TE Code : AP

    MICAFUNGIN SODIUM

    Brand Name : MYCAMINE

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : EQ 50MG BASE/VIAL

    Approval Date : 2005-03-16

    Application Number : 21506

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    04

    ASTELLAS

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    RLD : Yes

    TE Code : AP

    MICAFUNGIN SODIUM

    Brand Name : MYCAMINE

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

    Approval Date : 2006-06-27

    Application Number : 21506

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    05

    FUJISAWA HLTHCARE

    Japan
    Pharma, Lab & Chemical Expo
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    FUJISAWA HLTHCARE

    Japan
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    RLD :

    TE Code :

    MICAFUNGIN SODIUM

    Brand Name : MYCAMINE

    Dosage Form : INJECTABLE; INJECTION

    Dosage Strength : 50MG

    Approval Date :

    Application Number : 21754

    RX/OTC/DISCN :

    RLD :

    TE Code :

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    06

    FRESENIUS KABI USA

    U.S.A
    Pharma, Lab & Chemical Expo
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    FRESENIUS KABI USA

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    RLD : No

    TE Code : AP

    MICAFUNGIN SODIUM

    Brand Name : MICAFUNGIN SODIUM

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : EQ 50MG BASE/VIAL

    Approval Date : 2019-05-17

    Application Number : 207344

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    07

    FRESENIUS KABI USA

    U.S.A
    Pharma, Lab & Chemical Expo
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    FRESENIUS KABI USA

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    RLD : No

    TE Code : AP

    MICAFUNGIN SODIUM

    Brand Name : MICAFUNGIN SODIUM

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

    Approval Date : 2019-05-17

    Application Number : 207344

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    08

    TEVA PHARMS USA INC

    Israel
    Pharma, Lab & Chemical Expo
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    TEVA PHARMS USA INC

    Israel
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    RLD : Yes

    TE Code :

    MICAFUNGIN SODIUM

    Brand Name : MICAFUNGIN

    Dosage Form : POWDER;INTRAVENOUS

    Dosage Strength : EQ 50MG BASE/VIAL

    Approval Date : 2021-07-30

    Application Number : 212125

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    XELLIA PHARMS APS

    Denmark
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    XELLIA PHARMS APS

    Denmark
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    Pharma, Lab & Chemical Expo
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    RLD : No

    TE Code : AP

    MICAFUNGIN SODIUM

    Brand Name : MICAFUNGIN SODIUM

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : EQ 50MG BASE/VIAL

    Approval Date : 2021-06-02

    Application Number : 211713

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    10

    XELLIA PHARMS APS

    Denmark
    Pharma, Lab & Chemical Expo
    Not Confirmed
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    XELLIA PHARMS APS

    Denmark
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    Pharma, Lab & Chemical Expo
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    Flag Denmark
    Virtual Booth Virtual Booth
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    RLD : No

    TE Code : AP

    MICAFUNGIN SODIUM

    Brand Name : MICAFUNGIN SODIUM

    Dosage Form : INJECTABLE;INTRAVENOUS

    Dosage Strength : EQ 100MG BASE/VIAL

    Approval Date : 2021-06-02

    Application Number : 211713

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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